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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1814741Generated: October 30, 2026

Triethylamine → HCID 22498786, compound

https://huagongshe.com/reaction/1814741

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantPivalaldehydeHCID 12417—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactant2-Amino-1-(morpholin-4-yl)ethan-1-one--hydrogen chloride (1/1)HCID 12291814—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
ProductHCID 22498786HCID 2249878667%

Reaction Steps

To a stirred solution of the above 2-amino-1-morpholin-4-yl-ethanone hydrochloride (0.23 g, 1.3 mmol) in methylene chloride (4.0 mL) and triethylamine (0.19 mL, 1.4 mmol), 4 angstrom sieves (10 beads, pulverized to a powder) were added, followed by trimethylacetaldehyde (0.35 mL, 3.3 mmol) at room temperature, under argon. The resulting mixture was stirred at room temperature overnight after which time sodium triacetoxyborohydride (0.54 g, 2.6 mmol) was added. After 6 h, the solids were removed via filtration and washed with methylene chloride. The combined filtrates were concentrated and the remaining residue was diluted with EtOAc and water. The aqueous phase was lyophilized to give a white solid that was diluted with EtOAc. The solids were removed via filtration and washed with EtOAc. The combined organics were concentrated to give the crude product which was purified via silica gel flash chromatography eluting with 100% EtOAc, then 0.5% NH4OH/10% MeOH/EtOAc, flow rate 30 mL/min. The product-containing fractions were concentrated to give 0.18 g (67%) of 2-(2,2-dimethyl-propylamino)-1-morpholin-4yl-ethanone.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06878706B1
Source datasetuspto-grants-2005_04
ORD IDord-c377b1dd923a445a9ba22b41747fc979
Source noteuspto-grants-2005_04